A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293043



Internal ID20502261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11948051..11948376hg38UCSC Ensembl
chr17:11851368..11851693hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748019
Supporting Variants
Samples
Known GenesDNAH9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293043
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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